Thyroid Tonic NDC 44911-0309

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0309Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0309Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44911-0309-1	44911030901	30 mL in 1 BOTTLE, DROPPER (44911-0309-1)Marketed from Dec 1, 2015

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Thyroid Tonic
Generic name (nonproprietary): acacia arabica, oleum olea europaea, sesame oil, fucus vesiculosus 3x, iodium, thyroidinum (suis), baryta carbonica, borage oil, calcarea carbonica, natrum muriaticum, pulsatilla (pratensis), hydrofluoricum acidum
Active ingredients: Acacia — 2 [hp_X]/mLOlive oil — 2 [hp_X]/mLSesame oil — 2 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLIodine — 5 [hp_X]/mLThyroid — 6 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBorage oil — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLHydrofluoric acid — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Lipids (Chemical structure)Plant Proteins (Chemical structure)
Identifiers: Product ID 44911-0309_eaa6a1aa-e520-4ef8-b302-a6b9712ea08fSPL ID eaa6a1aa-e520-4ef8-b302-a6b9712ea08fSPL set ID aeca8e0e-12e6-44d0-a709-401d137f7cf3UNII 5C5403N26O, 6UYK2W1W1E, QX10HYY4QV, 535G2ABX9M, 9679TC07X4, 6RV024OAUQ, 6P669D8HQ8, F8XAG1755S, 2E32821G6I, 451W47IQ8X, 8E272251DI, RGL5YE86CZUPC 0363113701470
Pharmacologic class: Lipid Emulsion; Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911030901 followed by a unit qualifier and the quantity

Package 44911-0309-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 31, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve tightening of the throat, hoarseness, swollen joints, painful and dry cough in evening and at night.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)